Canonical Allele Identifier: CA1455108210
Gene: GABRA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.46971481T= , CM000666.2:g.46971481T= GRCh38
NC_000004.11:g.46973498T= , CM000666.1:g.46973498T= GRCh37
NC_000004.10:g.46668255T= NCBI36
NG_011809.1:g.27083A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264318.4:c.722-246A= MANE Select ENSP00000264318.3:n.722-246A=
ENST00000264318.3:c.722-246A= ENSP00000264318.3:n.722-246A=
ENST00000502874.1:c.*492-246A= ENSP00000424386.1:n.*492-246A=
ENST00000508560.5:c.*543-246A= ENSP00000425445.1:n.*543-246A=
ENST00000511523.5:c.*542+2751A= ENSP00000422152.1:n.*542+2751A=
NM_000809.3:c.722-246A= NP_000800.2:n.722-246A=
NM_001204266.1:c.665-246A= NP_001191195.1:n.665-246A=
NM_001204267.1:c.664+2751A= NP_001191196.1:n.664+2751A=
XM_011513677.1:c.721+2751A= XP_011511979.1:n.721+2751A=
NM_000809.4:c.722-246A= MANE Select NP_000800.2:n.722-246A=
NM_001204266.2:c.665-246A= NP_001191195.1:n.665-246A=
NM_001204267.2:c.664+2751A= NP_001191196.1:n.664+2751A=